Reflection phase microscopy using spatio-temporal coherence of light

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초록

Many disease states are associated with cellular biomechanical changes as markers. Label-free phase microscopes are used to quantify thermally driven interface fluctuations, which allow the deduction of important cellular rheological properties. Here, the spatio-temporal coherence of light was used to implement a high-speed reflection phase micro- scope with superior depth selectivity and higher phase sensitivity. Nanometric scale motion of cytoplasmic structures can be visualized with fine details and three-dimensional resolution. Specifically, the spontaneous fluctuation occurring on the nuclear membrane of a living cell was observed at video rate. By converting the reflection phase into displacement, the sensitivity in quantifying nuclear membrane fluctuation was found to be about one nanometer. A reflection phase microscope can potentially elucidate biomechanical mechanisms of pathological and physiological processes. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

키워드

DIGITAL HOLOGRAPHIC MICROSCOPY; SUPERCONTINUUM GENERATION; SPECKLE ILLUMINATION; PHOTONIC CRYSTAL; TOMOGRAPHY; DYNAMICS; CELLS; INTERFEROMETRY; DISEASE; FIBERS
제목
Reflection phase microscopy using spatio-temporal coherence of light
저자
Choi, Youngwoon; Hosseini, Poorya; Kang, Jeon Woong; Kang, Sungsam; Yang, Taeseok Daniel; Hyeon, Min Gyu; Kim, Beop-Min; So, Peter T. C.; Yaqoob, Zahid
DOI
10.1364/OPTICA.5.001468
발행일
2018-11-20
유형
Article
저널명
Optica
권
5
호
11
페이지
1468 ~ 1473